| Recruitment status | Completed |
| Unique ID issued by UMIN | UMIN000031552 |
| Receipt No. | R000035492 |
| Scientific Title | TR study of "A multicenter phase II study of eribulin monotherapy in patients with BRAF V600E mutant metastatic colorectal cancer (BRAVERY study)" |
| Date of disclosure of the study information | 2018/03/26 |
| Last modified on | 2021/09/24 (Ver. 14) |
| Basic information | ||
| Public title | TR study of "A multicenter phase II study of eribulin monotherapy in patients with BRAF V600E mutant metastatic colorectal cancer (BRAVERY study)" | |
| Acronym | BRAVERY TR | |
| Scientific Title | TR study of "A multicenter phase II study of eribulin monotherapy in patients with BRAF V600E mutant metastatic colorectal cancer (BRAVERY study)" | |
| Scientific Title:Acronym | BRAVERY TR | |
| Region |
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| Condition | |||
| Condition | BRAF V600E mutant metastatic colorectal cancer | ||
| Classification by specialty |
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| Classification by malignancy | Malignancy | ||
| Genomic information | YES | ||
| Objectives | |
| Narrative objectives1 | To explore biomarker relating to efficacy or resistance of eribulin in patients with BRAF V600E mutant metastatic colorectal cancer |
| Basic objectives2 | Efficacy |
| Basic objectives -Others | |
| Trial characteristics_1 | Exploratory |
| Trial characteristics_2 | |
| Developmental phase | Not applicable |
| Assessment | |
| Primary outcomes | cancer-related gene alteration, gene expression, microsatellite instability, BRAF mutant allele frequency |
| Key secondary outcomes | |
| Base | |
| Study type | Observational |
| Study design | |
| Basic design | |
| Randomization | |
| Randomization unit | |
| Blinding | |
| Control | |
| Stratification | |
| Dynamic allocation | |
| Institution consideration | |
| Blocking | |
| Concealment | |
| Intervention | |
| No. of arms | |
| Purpose of intervention | |
| Type of intervention | |
| Interventions/Control_1 | |
| Interventions/Control_2 | |
| Interventions/Control_3 | |
| Interventions/Control_4 | |
| Interventions/Control_5 | |
| Interventions/Control_6 | |
| Interventions/Control_7 | |
| Interventions/Control_8 | |
| Interventions/Control_9 | |
| Interventions/Control_10 | |
| Eligibility | ||||
| Age-lower limit |
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| Age-upper limit |
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| Gender | Male and Female | |||
| Key inclusion criteria | 1) Enrolled in the BRAVERY study
2) Written informed consent |
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| Key exclusion criteria | None | |||
| Target sample size | 42 | |||
| Research contact person | |||||||
| Name of lead principal investigator |
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| Organization | Aichi Cancer Center Hospital | ||||||
| Division name | Department of Clinical Oncology | ||||||
| Zip code | 464-8681 | ||||||
| Address | 1-1 Kanokoden, Chikusa-ku, Nagoya, 464-8681, Japan | ||||||
| TEL | 052-764-6111 | ||||||
| BRAVERY_core@east.ncc.go.jp | |||||||
| Public contact | |||||||
| Name of contact person |
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| Organization | Aichi Cancer Center Hospital | ||||||
| Division name | Department of Clinical Oncology | ||||||
| Zip code | 464-8681 | ||||||
| Address | 1-1 Kanokoden, Chikusa-ku, Nagoya, 464-8681, Japan | ||||||
| TEL | 052-764-6111 | ||||||
| Homepage URL | |||||||
| BRAVERY_core@east.ncc.go.jp | |||||||
| Sponsor | |
| Institute | Aichi Cancer Center Hospital |
| Institute | |
| Department | |
| Funding Source | |
| Organization | Self funding |
| Organization | |
| Division | |
| Category of Funding Organization | Self funding |
| Nationality of Funding Organization | Japan |
| Other related organizations | |
| Co-sponsor | |
| Name of secondary funder(s) | |
| IRB Contact (For public release) | |
| Organization | National Cancer Center Hospital Institutional Review Board |
| Address | Tsukiji 5-1-1, Chuo-ku, Tokyo |
| Tel | 04-7133-1111 |
| irboffice@east.ncc.go.jp | |
| Secondary IDs | |
| Secondary IDs | NO |
| Study ID_1 | |
| Org. issuing International ID_1 | |
| Study ID_2 | |
| Org. issuing International ID_2 | |
| IND to MHLW | |
| Institutions | |
| Institutions | 愛知県がんセンター(愛知県)、国立がん研究センター東病院(千葉県)、九州がんセンター(福岡県)、四国がんセンター(愛媛県)、北海道大学病院(北海道)、聖マリアンナ医科大学病院(神奈川県)、がん研究会有明病院(東京都)、大阪大学医学部附属病院(大阪府) |
| Other administrative information | |||||||
| Date of disclosure of the study information |
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| Related information | |
| URL releasing protocol | |
| Publication of results | Unpublished |
| Result | |
| URL related to results and publications | |
| Number of participants that the trial has enrolled | 27 |
| Results | |
| Results date posted | |
| Results Delayed | |
| Results Delay Reason | |
| Date of the first journal publication of results | |
| Baseline Characteristics | |
| Participant flow | |
| Adverse events | |
| Outcome measures | |
| Plan to share IPD | |
| IPD sharing Plan description | |
| Progress | |||||||
| Recruitment status | Completed | ||||||
| Date of protocol fixation |
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| Date of IRB |
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| Anticipated trial start date |
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| Last follow-up date |
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| Date of closure to data entry | |||||||
| Date trial data considered complete | |||||||
| Date analysis concluded | |||||||
| Other | |
| Other related information | This study is the additional study in UMIN ID:UMIN000031221. |
| Management information | |||||||
| Registered date |
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| Last modified on |
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| Link to view the page | |
| URL(English) | https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000035492 |